2DRX
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![BU of 2drx by Molmil](/molmil-images/mine/2drx) | Structure Analysis of (POG)4-(LOG)2-(POG)4 | Descriptor: | collagen like peptide | Authors: | Okuyama, K. | Deposit date: | 2006-06-16 | Release date: | 2007-04-24 | Last modified: | 2023-10-25 | Method: | X-RAY DIFFRACTION (1.4 Å) | Cite: | Unique side chain conformation of a leu residue in a triple-helical structure Biopolymers, 86, 2007
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2DRT
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![BU of 2drt by Molmil](/molmil-images/mine/2drt) | Structure Analysis of (POG)4-LOG-(POG)5 | Descriptor: | ETHANOL, collagen like peptide | Authors: | Okuyama, K. | Deposit date: | 2006-06-14 | Release date: | 2007-04-24 | Last modified: | 2023-10-25 | Method: | X-RAY DIFFRACTION (1.6 Å) | Cite: | Unique side chain conformation of a leu residue in a triple-helical structure Biopolymers, 86, 2007
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2G0G
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![BU of 2g0g by Molmil](/molmil-images/mine/2g0g) | Structure-based drug design of a novel family of PPAR partial agonists: virtual screening, x-ray crystallography and in vitro/in vivo biological activities | Descriptor: | 3-FLUORO-N-[1-(4-FLUOROPHENYL)-3-(2-THIENYL)-1H-PYRAZOL-5-YL]BENZENESULFONAMIDE, Peroxisome proliferator-activated receptor gamma | Authors: | Lu, I.L, Peng, Y.H, Huang, C.F, Lin, Y.T, Hsu, J.T.A, Wu, S.Y. | Deposit date: | 2006-02-13 | Release date: | 2006-05-16 | Last modified: | 2023-10-25 | Method: | X-RAY DIFFRACTION (2.54 Å) | Cite: | Structure-Based Drug Design of a Novel Family of PPARgamma Partial Agonists: Virtual Screening, X-ray Crystallography, and in Vitro/in Vivo Biological Activities J.Med.Chem., 49, 2006
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2G0H
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![BU of 2g0h by Molmil](/molmil-images/mine/2g0h) | Structure-based drug design of a novel family of PPAR partial agonists: virtual screening, x-ray crystallography and in vitro/in vivo biological activities | Descriptor: | N-[1-(4-FLUOROPHENYL)-3-(2-THIENYL)-1H-PYRAZOL-5-YL]-3,5-BIS(TRIFLUOROMETHYL)BENZENESULFONAMIDE, Peroxisome proliferator-activated receptor gamma | Authors: | Lu, I.L, Peng, Y.H, Huang, C.F, Lin, Y.T, Hsu, J.T.A, Wu, S.Y. | Deposit date: | 2006-02-13 | Release date: | 2006-05-16 | Last modified: | 2023-10-25 | Method: | X-RAY DIFFRACTION (2.3 Å) | Cite: | Structure-Based Drug Design of a Novel Family of PPARgamma Partial Agonists: Virtual Screening, X-ray Crystallography, and in Vitro/in Vivo Biological Activities J.Med.Chem., 49, 2006
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2GZ9
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![BU of 2gz9 by Molmil](/molmil-images/mine/2gz9) | |
2GZ8
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![BU of 2gz8 by Molmil](/molmil-images/mine/2gz8) | |
2GZ7
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![BU of 2gz7 by Molmil](/molmil-images/mine/2gz7) | |
7K3J
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![BU of 7k3j by Molmil](/molmil-images/mine/7k3j) | |
7K3K
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![BU of 7k3k by Molmil](/molmil-images/mine/7k3k) | |
7K3L
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![BU of 7k3l by Molmil](/molmil-images/mine/7k3l) | |